Efnb2tm1.1Henk/Efnb2+
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
|
normal
reproductive system phenotype |
J:91491
|
Efnb2tm1.1Henk/Efnb2+
involves: 129 * CD-1
|
abnormal endolymph physiology |
J:116671
|
circling |
J:116671
|
decreased posterior semicircular canal size |
J:116671
|
decreased superior semicircular canal size |
J:116671
|
head bobbing |
J:116671
|
small endolymphatic duct |
J:116671
|
Efnb2tm1.1Henk/Efnb2tm1.1Henk
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
|
abnormal angiogenesis |
J:91492
|
abnormal blood vessel morphology |
J:91492
|
abnormal cardiovascular development |
J:91492
|
abnormal heart morphology |
J:91492
|
abnormal vitelline vascular remodeling |
J:91492
|
abnormal vitelline vasculature morphology |
J:91492
|
decreased embryo size |
J:91492
|
embryonic growth retardation |
J:91492
|
embryonic lethality during organogenesis, complete penetrance |
J:91492
|
enlarged pericardium |
J:91492
|
Efnb2tm1.1Jwu/Efnb2tm1.1Jwu Tg(Lck-cre)I540Jxm/0
B6.Cg-Efnb2tm1.1Jwu Tg(Lck-cre)I540Jxm
|
normal
immune system phenotype |
J:178148
|
Efnb2tm1And/Efnb2tm1And
involves: 129S7/SvEvBrd
|
abnormal angiogenesis |
J:75288
|
abnormal cardinal vein morphology |
J:75288
|
abnormal endocardium morphology |
J:75288
|
abnormal heart ventricle morphology |
J:119151
|
abnormal myocardium layer morphology |
J:119151
|
abnormal vitelline vasculature morphology |
J:75288
|
absent myocardial trabeculae |
J:75288
|
normal
cardiovascular system phenotype |
J:75288
|
embryonic growth retardation |
J:75288
|
embryonic lethality during organogenesis, complete penetrance |
J:75288
|
enlarged heart |
J:75288
|
Efnb2tm1And/Efnb2tm1And
involves: 129S7/SvEvBrd * C57BL/6
|
abnormal angiogenesis |
J:74909
|
abnormal anterior cardinal vein morphology |
J:74909
|
abnormal developmental vascular remodeling |
J:74909
|
abnormal heart looping |
J:74909
|
abnormal intersomitic vessel morphology |
J:74909
|
abnormal vitelline vasculature morphology |
J:74909
|
absent myocardial trabeculae |
J:74909
|
decreased embryo size |
J:74909
|
enlarged heart |
J:74909
|
Efnb2tm1And/Efnb2tm2And Tg(Tek-cre)12Flv/0
involves: 129S7/SvEvBrd * C57BL/6
|
abnormal angiogenesis |
J:74909
|
abnormal developmental vascular remodeling |
J:74909
|
abnormal heart looping |
J:74909
|
abnormal intersomitic vessel morphology |
J:74909
|
abnormal vascular development |
J:74909
|
abnormal vitelline vasculature morphology |
J:74909
|
absent myocardial trabeculae |
J:74909
|
decreased embryo size |
J:74909
|
embryonic growth arrest |
J:74909
|
embryonic lethality during organogenesis, complete penetrance |
J:74909
|
enlarged heart |
J:74909
|
Efnb2tm1Henk/Efnb2+
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
|
abnormal anogenital distance |
J:91491
|
abnormal penis morphology |
J:91491
|
abnormal septation of the cloaca |
J:91491
|
hypospadia |
J:91491
|
male infertility |
J:91491
|
splayed clitoris |
J:91491
|
Efnb2tm1Henk/Efnb2+
involves: 129 * CD-1
|
abnormal endolymph physiology |
J:116671
|
abnormal vestibular endolymph ionic homeostasis |
J:116671
|
abnormal vestibular endolymph physiology |
J:116671
|
circling |
J:116671
|
cleft palate |
J:173636
|
decreased posterior semicircular canal size |
J:116671
|
decreased superior semicircular canal size |
J:116671
|
head bobbing |
J:116671
|
small endolymphatic duct |
J:116671
|
Efnb2tm1Henk/Efnb2+
Not Specified
|
abnormal axon morphology |
J:176056
|
Efnb2tm1Henk/Efnb2tm1Henk
either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1)
|
abnormal anterior commissure pars posterior morphology |
J:91492
|
abnormal axon guidance |
J:91492
|
abnormal heart valve morphology |
J:91492
|
abnormal septation of the cloaca |
J:91491
|
abnormal urethra morphology |
J:91491
|
anal atresia |
J:91491
|
aortic valve hyperplasia |
J:91492
|
normal
cardiovascular system phenotype |
J:91492
|
embryonic lethality between implantation and placentation, incomplete penetrance |
J:91492
|
enlarged aortic valve |
J:91492
|
enlarged pulmonary valve |
J:91492
|
hypospadia |
J:91491
|
neonatal lethality, complete penetrance |
J:91491,
J:91492
|
persistent cloaca |
J:91491
|
pulmonary valve hyperplasia |
J:91492
|
splayed clitoris |
J:91491
|
thick aortic valve |
J:91492
|
thick mitral valve cusps |
J:91492
|
thick pulmonary valve |
J:91492
|
Efnb2tm1Henk/Efnb2tm1Henk
involves: 129 * CD-1
|
abnormal common crus morphology |
J:116671
|
abnormal semicircular canal morphology |
J:116671
|
cleft palate |
J:173636
|
decreased endolymph production |
J:116671
|
dilated endolymphatic duct |
J:116671
|
dilated endolymphatic sac |
J:116671
|
neonatal lethality, complete penetrance |
J:173636
|
tracheoesophageal fistula |
J:173636
|
Efnb2tm1Henk/Efnb2tm1Henk Tbx4tm1(cre)Tmj/Tbx4+
involves: 129S1/Sv * 129X1/SvJ
|
normal
nervous system phenotype |
J:176643
|
Efnb2tm1Henk/Efnb2tm2.1Henk
involves: 129 * CD-1
|
hypospadia |
J:173636
|
Efnb2tm1Henk/Efnb2tm3.1Henk
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
abnormal axon morphology |
J:176056
|
hypospadia |
J:173636
|
Efnb2tm1Kln/Efnb2tm1Kln
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
abnormal angiogenesis |
J:67296
|
abnormal cardinal vein morphology |
J:67296
|
abnormal intersomitic vessel morphology |
J:67296
|
abnormal neural crest cell migration |
J:67296
|
abnormal second pharyngeal arch morphology |
J:67296
|
absent pharyngeal arch arteries |
J:67296
|
absent second pharyngeal arch |
J:67296
|
normal
embryo phenotype |
J:67296
|
embryonic growth retardation |
J:67296
|
embryonic lethality during organogenesis, complete penetrance |
J:67296
|
small second pharyngeal arch |
J:67296
|
Efnb2tm2.1Henk/Efnb2tm2.1Henk
involves: 129 * CD-1
|
normal
digestive/alimentary phenotype |
J:173636
|
premature death |
J:173636
|
Efnb2tm2.1Kln/Efnb2tm2.1Kln
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
no abnormal phenotype detected |
J:67296
|
Efnb2tm2And/Efnb2tm2And Tg(CAG-cre/Esr1*)1Egwa/0
involves: 129S7/SvEvBrd * C57BL/6 * DBA/2
|
abnormal angiogenesis |
J:157054
|
abnormal skin physiology |
J:157054
|
flaky skin |
J:157054
|
hyperkeratosis |
J:157054
|
normal
integument phenotype |
J:157054
|
postnatal growth retardation |
J:157054
|
postnatal lethality, complete penetrance |
J:157054
|
retarded hair growth |
J:157054
|
small hair follicles |
J:157054
|
thick epidermis |
J:157054
|
thin hypodermis |
J:157054
|
Efnb2tm2Sor/Efnb2tm2Sor
involves: 129S4/SvJaeSor
|
embryonic lethality, complete penetrance |
J:115952
|
Efnb2tm2Sor/Efnb2tm2Sor
involves: 129S4/SvJaeSor * C57BL/6J
|
abnormal cranial neural crest cell migration |
J:143845
|
abnormal dorsal-ventral polarity of the somites |
J:143845
|
abnormal rostral-caudal patterning of the somites |
J:143845
|
abnormal somite development |
J:143845
|
abnormal trunk neural crest cell migration |
J:143845
|
decreased cranial neural crest cell number |
J:143845
|
embryonic lethality during organogenesis, complete penetrance |
J:143845
|
increased cranial neural crest cell apoptosis |
J:143845
|
small first pharyngeal arch |
J:143845
|
small trigeminal ganglion |
J:143845
|
Efnb2tm3.1Henk/Efnb2+
involves: 129S1/Sv * 129X1/SvJ
|
abnormal axon morphology |
J:176056
|
Efnb2tm3.1Henk/Efnb2tm3.1Henk
involves: 129S1/Sv * 129X1/SvJ * CD-1
|
normal
digestive/alimentary phenotype |
J:173636
|
premature death |
J:173636
|
Efnb2tm3.1Kln/Efnb2tm3.1Kln
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
|
abnormal anterior cardinal vein morphology |
J:67296
|
abnormal intersomitic vessel morphology |
J:67296
|
abnormal vitelline vascular remodeling |
J:67296
|
distended pericardium |
J:67296
|
normal
embryo phenotype |
J:67296
|
embryonic growth retardation |
J:67296
|
embryonic lethality during organogenesis, complete penetrance |
J:67296
|
small pharyngeal arch |
J:67296
|
Efnb2tm4Kln/Efnb2tm4Kln Tg(Camk2a-cre)159Kln/0
involves: 129P2/OlaHsd * C57BL/6
|
normal
behavior/neurological phenotype |
J:87398
|
normal
nervous system phenotype |
J:87398
|
reduced long-term potentiation |
J:87398
|
Efnb2tm4Kln/Efnb2tm4Kln Tg(Nes-cre)1Kln/0
involves: 129P2/OlaHsd * C57BL/6
|
abnormal long-term depression |
J:87398
|
normal
nervous system phenotype |
J:87398
|
Efnb2tm5Kln/Efnb2tm5Kln
involves: C57BL/6
|
chylothorax |
J:95885
|
postnatal lethality, complete penetrance |
J:95885
|